Discussing Endogenous NO•/HNO Interconversion Aided by Phenolic Drugs and Vitamins

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The reduction of NO• to HNO/NO- under biologically compatible conditions has always been thought as unlikely, mostly because of the negative reduction potential: E°(NO•,H+/HNO) = -0.55 V vs NHE at physiological pH. Nonetheless, during the past decade, several works hinted at the possible NO-to-HNO c...

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Autor principal: Hamer, M.
Otros Autores: Suarez, S.A, Neuman, N.I, Alvarez, L., Muñoz, M., Marti, M.A, Doctorovich, F.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: American Chemical Society 2015
Acceso en línea:Registro en Scopus
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100 1 |a Hamer, M. 
245 1 0 |a Discussing Endogenous NO•/HNO Interconversion Aided by Phenolic Drugs and Vitamins 
260 |b American Chemical Society  |c 2015 
270 1 0 |m Marti, M.A.; Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. II, Argentina 
506 |2 openaire  |e Política editorial 
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520 3 |a The reduction of NO• to HNO/NO- under biologically compatible conditions has always been thought as unlikely, mostly because of the negative reduction potential: E°(NO•,H+/HNO) = -0.55 V vs NHE at physiological pH. Nonetheless, during the past decade, several works hinted at the possible NO-to-HNO conversion mediated by moderate biological reductants. Very recently, we have shown that the reaction of NO• with ascorbate and aromatic alcohols occurs through a proton-coupled nucleophilic attack (PCNA) of the alcohol to NO•, yielding an intermediate RO-N(H)O• species, which further decomposes to release HNO. For the present work, we decided to inspect whether other common biological aromatic alcohols obtained from foods, such as Vitamin E, or used as over-the-counter drugs, like aspirin, are able to undergo the reaction. The positive results suggest that the conversion of NO to HNO could occur far more commonly than previously expected. Taking these as the starting point, we set to review our and other groups' previous reports on the possible NO-to-HNO conversion mediated by biological compounds including phenolic drugs and vitamins, as well as several thiol-bearing compounds. Analysis of revised data prompted us to ask ourselves the following key questions: What are the most likely physio/pathological conditions for NO•-to-HNO conversion to take place? Which effects usually attributed to NO• are indeed mediated by HNO? These inquiries are discussed in the context of 2 decades of NO and HNO research. © 2015 American Chemical Society.  |l eng 
593 |a Departamento de Química Analítica y Fisicoquímica, Facultad de Farmacia y Bioquímica (IQUIFIB-CONICET), Universidad de Buenos Aires, Junin 956Buenos Aires, Argentina 
593 |a Gerencia de Investigación y Aplicaciones, Centro Atómico Constituyentes, Comisión Nacional de Energía AtómicaBuenos Aires, Argentina 
593 |a Departamento de Química Inorgánica, Analítica y Química Física, Facultad de Ciencias Exactas y Naturales (INQUIMAE-CONICET), Universidad de Buenos Aires, Ciudad UniversitariaBuenos Aires, Argentina 
593 |a Departamento de Física, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Ciudad Universitaria, Paraje El Pozo, Santa Fe, Argentina 
593 |a Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Ciudad Universitaria, Pab. IIBuenos Aires, Argentina 
690 1 0 |a ACETYLSALICYLIC ACID 
690 1 0 |a ALPHA TOCOPHEROL 
690 1 0 |a FREE RADICAL 
690 1 0 |a NITROGEN OXIDE 
690 1 0 |a NITROXYL 
690 1 0 |a PHENOL DERIVATIVE 
690 1 0 |a CHEMICAL STRUCTURE 
690 1 0 |a CHEMISTRY 
690 1 0 |a ASPIRIN 
690 1 0 |a FREE RADICALS 
690 1 0 |a MOLECULAR STRUCTURE 
690 1 0 |a NITROGEN OXIDES 
690 1 0 |a PHENOLS 
690 1 0 |a VITAMIN E 
700 1 |a Suarez, S.A. 
700 1 |a Neuman, N.I. 
700 1 |a Alvarez, L. 
700 1 |a Muñoz, M. 
700 1 |a Marti, M.A. 
700 1 |a Doctorovich, F. 
773 0 |d American Chemical Society, 2015  |g v. 54  |h pp. 9342-9350  |k n. 19  |p Inorg. Chem.  |x 00201669  |w (AR-BaUEN)CENRE-60  |t Inorganic Chemistry 
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